Cap polyposis
Synonyms: Cap inflammatory polyposis · Eroded polypoid hyperplasia · Inflammatory myoglandular polyps · Polypoid prolapsing folds
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Elderly
- Status
- active
A rare colorectal disease characterized by multiple inflammatory polyps that predominantly affect the rectosigmoid area and that manifests primarily as rectal bleeding with abnormal transit, constipation and diarrhea.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cap polyposis | Cap inflammatory polyposis · Eroded polypoid hyperplasia · Inflammatory myoglandular polyps · Polypoid prolapsing folds |
| fr | Cap polypose | Hyperplasie polypoïde érodée · Polype myoglandulaire inflammatoire |
| de | Kappen-Polypose | Cap-Polypose · Polypen, entzündliche myoglanduläre · Polypoide Hyperplasie, erodierte |
| es | Poliposis con capuchón | Hiperplasia polipoide erosionada · Pliegues polipoides prolapsados · Pliegues polipoides prolapsantes · Pólipos inflamatorios mioglandulares · Pólipos mioglandulares inflamatorios |
| it | Poliposi a cappuccio | |
| nl | Cap polyposis | Geërodeerde polypoïde hyperplasie · Inflammatoire myoglandulaire poliepen · Polypoïde verzakkende vouwen |
| pt | Polipose Cap | |
| pl | Polipowatość z polipami typu "cap" (czapeczką fibrynową) | Eroded polypoid hyperplasia · Polipy zapalne mięsniowo-gruczołowe · Polypoid prolapsing folds |
| cs | Erodovaná polypoidní hyperplázie | Zánětlivé myoglandulární polypy · Prolabující polypoidní řasy |
| uk | Ковпачковий поліпоз | Запальний поліпоз кришечки · Ерозована поліпозна гіперплазія · Запальні міогландулярні поліпи · Поліпоїдні складки, що випинаються |
| zh | 帽状息肉病 | 炎性肌腺性息肉 |
| tr | Kapak polipozu | Polipoid sarkan kıvrımlar · Cap inflamatuar polipoz · Aşınmış polipoid hiperplazi · İnflamatuar miyoglandüler polipler |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D12.6 | NTBT | attributed | validated |
| ICD-11 | 2E92.40 | NTBT | index | validated |
| MONDO | 0015565 | E | validated | |
| UMLS | C4303971 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:117569Rare intestinal disease
rare gastroenterological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 67 cases | Worldwide | Case(s) | Validated | 24949613[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | ORPHANET_24949613[PMID] |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
HPO phenotypes
8 annotations · validated 2016-10-17| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Obligate (100%) | ||
| HP:0200063 | Colorectal polyposis | |
| Very frequent (99-80%) | ||
| HP:0002027 | Abdominal pain | |
| HP:0002582 | Atrophic gastritis | |
| HP:0002019 | Constipation | |
| HP:0002573 | Hematochezia | |
| Frequent (79-30%) | ||
| HP:0003270 | Abdominal distention | |
| HP:0002014 | Diarrhea | |
| HP:0001824 | Weight loss | |
Run the differential on the 5 obligate / very frequent terms
Annotation source: 23416507[PMID]_22333383[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/160148
- This record as JSON: /data/d/160148.json